Bad taste in mouth : Anyone with PD get... - Cure Parkinson's

Cure Parkinson's

25,881 members27,179 posts

Bad taste in mouth

Tiger101 profile image
7 Replies

Anyone with PD get bad taste in mouth if so what can be done?

Written by
Tiger101 profile image
Tiger101
To view profiles and participate in discussions please or .
Read more about...
7 Replies

Sour Jacks candy

parkie13 profile image
parkie13

Do you have any clue what is causing it? Medication? Is it coming from your mouth or from your stomach? I'm a firm believer in using 3% hydrogen peroxide in a brown bottle that you buy in a grocery store. I have been using it full strength but if it bothers you you can't diluted with water 50/50. It does the wonderful job killing the bacteria in your mouth.

Tiger101 profile image
Tiger101 in reply to parkie13

Not sure. It’s going along with his loss of taste and smell. He is newly diagnosed with PD and has started Rytary.

alexask profile image
alexask in reply to Tiger101

Mannitol restores sense of smell in 80% that have tried it (according to Clinicrowd), so may help with this. It also helps with constipation, so if this is also a problem it is worth a try.

Tiger101 profile image
Tiger101 in reply to alexask

Awesome thanks! My husband has terrible constipation. Maybe goes once a week. He is newly diagnosed so they don't want to introduce anything until he gets used to the Rytary. This is definitely on my list!

alexask profile image
alexask in reply to Tiger101

Cool. You can look at my profile for my full regime, but in a nutshell I would recommend - a level tablespoon of Mannitol each morning - ideally in Coffee together with Coconut oil and a low carb breakfast - e.g Bacon and eggs - maybe with one slice of toast. Or a cheese omelette. Take some curcumin with pepper at the same time.

To try and get him moving - apples - eat the core too and crunch the pips as there is some good stuff in there too. Obviously prunes would work too.

I had terrible constipation (from someone who was previously very regular), but this really sorted it.

And exercise as much and varied as possible.

alexask profile image
alexask in reply to alexask

I am 70 kg. With Mannitol you basically need to balance the amount so you become more regular without spending your entire time on the toilet. And not so much in the evening - I got reflux, which may or may not be related. So I don't really have any after about 3pm.

Lot's of people regain their sense of smell with Mannitol, but not much else - but for the early stages I think it can make a major difference in reversing some even many of the symptoms.

You may also like...

Taste and smell and stamina.

My sense of smell and taste has improved 25% in the last few month. I think my pd is reversing I...

A taste of my own medicine

about telling myself I can And you know what. It took a bit of work, but I can play it again....

Mannitol and sense of Taste/Smell

and it had one affect on my sense of taste - I found the taste of wine very chemically and...

Dry mouth, dry eyes and dry skin

Has anyone noticed having dry eye, dry mouth and dry skin since being diagnosed with Parkinson’s?...

Calcium - good or bad?

o-s-the-key/cid/1375858 So now I’m confused. Can anyone clarify whether we should be avoiding...